600 Research And Development jobs in Bangalore

• Assist senior scientists in designing and executing experiments related to biochemistry and molecular biology.
• Perform laboratory procedures such as cell culture, PCR, Western blotting, and protein purification.
• Collect, record, and analyze experimental data using appropriate software tools.
• Maintain detailed and accurate laboratory notebooks.
• Conduct literature reviews to support research projects.
• Prepare technical reports and present findings to the research team.
• Ensure compliance with all laboratory safety protocols and procedures.
• Contribute to troubleshooting experimental challenges and proposing solutions.
• Collaborate effectively with other members of the research team in a virtual setting.
• Manage laboratory supplies and inventory as needed.
• Learn and apply new scientific techniques and methodologies.

Company Description

At Vellichor Media, we are a team of passionate and creative designers, writers, and developers. We focus on enhancing the marketing operations of our clients. By analyzing their unique requirements, we help them step into the digital age and deliver the right solutions to meet their needs.

Role Description

This is a full-time on-site role for a Market Research Executive located in Bengaluru. The Market Research Executive will be responsible for conducting market research, analyzing market data, designing questionnaires, and providing actionable insights. The role involves gathering and interpreting data, preparing reports, and communicating findings to stakeholders.

Qualifications

• Strong Market Research and Market Analysis skills
• Excellent Analytical Skills
• Effective Communication skills
• Experience in Questionnaire Design
• Attention to detail and problem-solving abilities
• Bachelor's degree in Marketing, Business, or related field is preferred
• Ability to work collaboratively in a team environment

Experience: ONLY Freshers

• Conduct comprehensive monitoring visits to clinical trial sites to assess compliance with protocols, SOPs, and regulatory guidelines.
• Verify accuracy and completeness of data recorded in CRFs against source documents.
• Manage investigational product accountability and ensure proper storage and dispensing.
• Identify, document, and report adverse events and serious adverse events.
• Build and maintain strong working relationships with investigators, site staff, and study sponsors.
• Provide training and support to site personnel on study procedures and regulatory requirements.
• Prepare monitoring reports and ensure timely submission of all required documentation.
• Participate in site selection, initiation, and close-out activities.
• Ensure all trial-related activities are conducted in accordance with Good Clinical Practice (GCP) guidelines.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Master's degree preferred.
• Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
• Thorough understanding of ICH-GCP guidelines and local regulatory requirements.
• Proven experience in monitoring clinical trials across various therapeutic areas.
• Excellent communication, interpersonal, and organizational skills.
• Ability to work independently, manage time effectively, and meet deadlines.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Strong problem-solving and analytical abilities.
• Willingness to travel for essential project meetings or site visits as needed.

• Perform site selection, initiation, monitoring, and close-out visits in accordance with protocol, GCP, and regulatory requirements.
• Ensure accurate and timely source data verification and entry into clinical databases.
• Monitor study conduct to ensure compliance with protocol, SOPs, GCP, and applicable regulations.
• Manage a portfolio of clinical trial sites, building strong relationships with investigators and site staff.
• Train and mentor junior CRAs and site personnel on study-related procedures.
• Oversee the drug accountability process at investigator sites.
• Ensure that regulatory documentation is complete, accurate, and maintained at each site.
• Identify, report, and escalate potential protocol deviations or non-compliance issues.
• Collaborate with internal study teams, including project managers, data managers, and medical monitors.
• Prepare monitoring visit reports and follow up on action items with investigator sites.
• Contribute to the development of study protocols, case report forms (CRFs), and other study documents.
• Stay current with regulatory guidelines and industry best practices in clinical research.
• Participate in team meetings and provide updates on site progress and challenges.
• Ensure timely resolution of site-specific issues and queries.
• Promote a culture of quality and compliance throughout the clinical trial process.

• Minimum of 4 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Proven experience in monitoring various phases of clinical trials.
• Excellent monitoring skills, including source data verification and query resolution.
• Strong interpersonal and communication skills, with the ability to build rapport with site personnel.
• Demonstrated ability to manage multiple sites and prioritize tasks effectively.
• Proficiency in Electronic Data Capture (EDC) systems and clinical trial management systems (CTMS).
• Ability to travel as required for site visits.
• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Strong analytical and problem-solving skills.
• Detail-oriented with excellent organizational skills.

• Conduct site visits (pre-study, initiation, monitoring, close-out) to ensure adherence to protocols and regulations.
• Verify clinical trial data accuracy and completeness, ensuring compliance with GCP and ICH guidelines.
• Manage relationships with principal investigators and study site personnel.
• Train and mentor junior CRAs on trial procedures and best practices.
• Prepare and present study progress reports to project management and stakeholders.
• Identify, assess, and resolve site-level issues and risks.
• Ensure timely submission of essential documents and regulatory filings.
• Contribute to the development and revision of study protocols and Standard Operating Procedures (SOPs).
• Maintain comprehensive and accurate study documentation.

• Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, or a related field.
• Minimum of 5 years of experience as a Clinical Research Associate.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements (e.g., FDA, EMA).
• Proven experience in monitoring clinical trials across various therapeutic areas.
• Excellent communication, interpersonal, and negotiation skills.
• Strong analytical and problem-solving abilities.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel as required for site visits.
• Demonstrated leadership potential and mentoring capabilities.

• Perform site selection, initiation, monitoring, and close-out visits.
• Ensure compliance with study protocols, SOPs, and GCP guidelines.
• Monitor clinical trial data for accuracy, completeness, and integrity.
• Verify source documentation and investigational product accountability.
• Identify and resolve site-level issues promptly.
• Build and maintain strong relationships with investigators and site staff.
• Train site personnel on study procedures.
• Prepare monitoring visit reports and action items.
• Ensure timely submission of regulatory documents.
• Contribute to study team meetings and discussions.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
• Minimum of 5-8 years of experience as a Clinical Research Associate.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience in multiple therapeutic areas is desirable.
• Strong monitoring skills and understanding of clinical trial processes.
• Excellent analytical, problem-solving, and organizational abilities.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Effective communication, interpersonal, and negotiation skills.

• Lead the development and optimization of various drug formulations (e.g., oral solids, liquids, injectables).
• Design and execute pre-formulation studies to understand drug properties.
• Conduct experiments to evaluate excipient compatibility and selection.
• Develop and validate analytical methods for formulation characterization.
• Oversee the scale-up of formulations from laboratory to pilot plant scale.
• Ensure all development activities comply with regulatory guidelines (e.g., FDA, EMA).
• Collaborate with analytical, process development, and regulatory teams.
• Prepare comprehensive development reports and documentation for regulatory submissions.
• Mentor junior scientists and contribute to a culture of scientific excellence.
• Stay current with scientific literature and emerging technologies in pharmaceutical formulation.

• Ph.D. or Master's degree in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related field.
• 5+ years of hands-on experience in pharmaceutical formulation development.
• Proven expertise in oral solid dosage forms, liquid formulations, or sterile products.
• Strong knowledge of drug delivery systems and excipient functionalities.
• Experience with formulation characterization techniques and analytical method development.
• Familiarity with GMP guidelines and regulatory submission requirements.
• Excellent scientific writing and presentation skills.
• Strong problem-solving and critical thinking abilities.
• Ability to work effectively in a hybrid R&D environment.
• Leadership potential and ability to mentor junior team members.

• Conduct site selection, initiation, monitoring, and close-out visits for clinical trials.
• Ensure compliance with study protocols, SOPs, and regulatory requirements (GCP, FDA, EMA).
• Verify the accuracy and completeness of clinical data at study sites.
• Assess patient safety and ensure adherence to ethical standards.
• Train and support investigators and study staff on trial procedures.
• Manage study documentation and regulatory binders.
• Identify, track, and resolve site-specific issues and deviations.
• Communicate effectively with study sites, internal teams, and sponsors.
• Prepare and present monitoring visit reports.
• Contribute to the development of study protocols and CRFs as needed.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
• Minimum of 5 years of experience as a Clinical Research Associate, with a significant focus on oncology trials.
• In-depth knowledge of GCP, FDA regulations, and ICH guidelines.
• Proven experience in site monitoring and data verification.
• Excellent analytical, organizational, and problem-solving skills.
• Strong communication, interpersonal, and negotiation abilities.
• Ability to travel to study sites as required.
• Experience with electronic data capture (EDC) systems.